Ndam Nicaise Tuikue, Deloron Philippe
UR 010, Laboratoire de Parasitologie, Institut de Recherche pour le Développement, Université Paris Descartes, IFR 71, 75006 Paris, France.
J Biomed Biotechnol. 2007;2007(5):43785. doi: 10.1155/2007/43785.
Cytoadherence of Plasmodium-falciparum-parasitized red blood cells (PRBCs) to host receptors is the key phenomenon in the pathological process of the malaria disease. Some of these interactions can originate poor outcomes responsible for 1 to 3 million annual deaths mostly occurring among children in sub-Saharan Africa. Pregnancy-associated malaria (PAM) represents an important exception of the disease occurring at adulthood in malaria endemic settings. Consequences of this are shared between the mother (maternal anemia) and the baby (low birth weight and infant mortality). Demonstrating that parasites causing PAM express specific variant surface antigens (VSA(PAM)), including the P. falciparum erythrocyte membrane protein 1 (P f EMP1) variant VAR2CSA, that are targets for protective immunity has strengthened the possibility for the development of PAM-specific vaccine. In this paper, we review the molecular basis of malaria pathogenesis attributable to the erythrocyte stages of the parasites, and findings supporting potential anti-PAM vaccine components evidenced in PAM.
恶性疟原虫寄生的红细胞(PRBCs)与宿主受体的细胞黏附是疟疾疾病病理过程中的关键现象。其中一些相互作用可能导致不良后果,每年造成100万至300万人死亡,这些死亡大多发生在撒哈拉以南非洲的儿童中。妊娠相关疟疾(PAM)是疟疾流行地区成年期发生的该疾病的一个重要例外情况。其后果由母亲(产妇贫血)和婴儿(低出生体重和婴儿死亡率)共同承担。有证据表明,导致PAM的寄生虫表达特定的变异表面抗原(VSA(PAM)),包括恶性疟原虫红细胞膜蛋白1(Pf EMP1)变体VAR2CSA,这些是保护性免疫的靶点,这增强了开发PAM特异性疫苗的可能性。在本文中,我们综述了寄生虫红细胞阶段所致疟疾发病机制的分子基础,以及支持PAM中潜在抗PAM疫苗成分的研究结果。